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Cairn Diagnostics

Country not established FDA establishment FEI 3009091796

Devices
0
Registrations
FDA
FDA recalls
1

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3009091796
Address
105 WESTPARK DR STE 150, Brentwood, TN, 37027

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 1
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0
  • 2021

    • 8 Jan 2021 Z-1128-2021 Class II Terminated Potential for false negative diagnosis of gastroparesis. Certain GEBT kits containing 13C-Spirulina elicit unusually high 13CO2-excretion rates Distribution: US Nationwide distribution in the states of GA, NY, MI, CA, KS, NC.

This is an FDA establishment record without devices in deviCERTS.